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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054928inversion1nstd229human GRCh38 chr4: 56,642,680-60,318,047 , GRCh37.p13 chr4: 57,508,846-61,183,765 LOC107986228, POLR2B, 26 more genes
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6735035copy number variation1nstd229human GRCh38 chr4: 57,427,620-57,427,691 , GRCh37.p13 chr4: 58,293,786-58,293,857 LINC02380
    nsv6734175copy number variation1nstd229human GRCh38 chr4: 57,435,967-57,442,739 , GRCh37.p13 chr4: 58,302,133-58,308,905 LINC02380
    nsv6730250copy number variation1nstd229human GRCh38 chr4: 57,345,524-57,827,985 , GRCh37.p13 chr4: 58,211,690-58,694,151 RPS26P24, LINC02380
    nsv6728672copy number variation1nstd229human GRCh38 chr4: 57,426,483-57,446,276 , GRCh37.p13 chr4: 58,292,649-58,312,442 LINC02380
    nsv6727140copy number variation1nstd229human GRCh38 chr4: 57,442,416-57,448,972 , GRCh37.p13 chr4: 58,308,582-58,315,138 LINC02380
    nsv6723076copy number variation1nstd229human GRCh38 chr4: 57,431,189-57,431,468 , GRCh37.p13 chr4: 58,297,355-58,297,634 LINC02380
    nsv6721809copy number variation1nstd229human GRCh38 chr4: 57,430,806-57,436,760 , GRCh37.p13 chr4: 58,296,972-58,302,926 LINC02380
    nsv6721754copy number variation1nstd229human GRCh38 chr4: 57,426,679-58,230,973 , GRCh37.p13 chr4: 58,292,845-59,097,139 SRIP1, LINC02380, 1 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6629932copy number variation1nstd224human GRCh37 chr4: 58,279,415-58,968,465 , GRCh38.p12 chr4: 57,413,249-58,102,299 SRIP1, LINC02380, 1 more genes
    nsv6629877copy number variation1nstd224human GRCh37 chr4: 58,139,970-58,655,901 , GRCh38.p12 chr4: 57,273,804-57,789,735 LINC02380, RPS26P24
    nsv6629876copy number variation1nstd224human GRCh37 chr4: 58,136,668-58,491,683 , GRCh38.p12 chr4: 57,270,502-57,625,517 LINC02380, RPS26P24
    nsv6575116inversion1nstd223human GRCh38 chr4: 56,642,680-60,318,047 , GRCh37.p13 chr4: 57,508,846-61,183,765 LOC105377666, RN7SL357P, 26 more genes
    nsv6392930copy number variation1nstd223human GRCh38 chr4: 57,428,991-57,429,681 , GRCh37.p13 chr4: 58,295,157-58,295,847 LINC02380
    nsv6392630copy number variation1nstd223human GRCh38 chr4: 57,037,036-57,884,522 , GRCh37.p13 chr4: 57,903,202-58,750,688 IGFBP7, RPS26P24, 5 more genes
    nsv6386011copy number variation1nstd223human GRCh38 chr4: 57,452,463-57,452,847 , GRCh37.p13 chr4: 58,318,629-58,319,013 LINC02380
    nsv6382848copy number variation1nstd223human GRCh38 chr4: 57,430,138-57,431,511 , GRCh37.p13 chr4: 58,296,304-58,297,677 LINC02380
    nsv6382146copy number variation1nstd223human GRCh38 chr4: 57,272,910-57,701,197 , GRCh37.p13 chr4: 58,139,076-58,567,363 RPS26P24, LINC02380
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